Canonical Allele Identifier: CA383823842

Gene: A2ML1

Linked Data

• MyVariant Identifiers: chr12:g.8991811G>A (hg19) ; chr12:g.8839215G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8839215G>A , CM000674.2:g.8839215G>A	GRCh38
NC_000012.11:g.8991811G>A , CM000674.1:g.8991811G>A	GRCh37
NC_000012.10:g.8883078G>A	NCBI36
NG_042857.1:g.21744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299698.12:c.1073G>A MANE Select	ENSP00000299698.7:p.Ser358Asn
ENST00000299698.11:c.1073G>A	ENSP00000299698.7:p.Ser358Asn
NM_144670.4:c.1073G>A	NP_653271.2:p.Ser358Asn
NM_144670.5:c.1073G>A	NP_653271.2:p.Ser358Asn
XM_011520566.1:c.1073G>A	XP_011518868.1:p.Ser358Asn
XM_011520567.1:c.1073G>A	XP_011518869.1:p.Ser358Asn
XR_931275.1:n.1171G>A
XM_011520566.2:c.1073G>A	XP_011518868.1:p.Ser358Asn
XM_011520567.2:c.1073G>A	XP_011518869.1:p.Ser358Asn
XM_017018868.1:c.1073G>A	XP_016874357.1:p.Ser358Asn
XM_017018869.1:c.1073G>A	XP_016874358.1:p.Ser358Asn
XM_017018870.1:c.1073G>A	XP_016874359.1:p.Ser358Asn
XR_001748594.1:n.1171G>A
NM_144670.6:c.1073G>A MANE Select	NP_653271.3:p.Ser358Asn